A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4734152



Internal ID20510086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:111545638..111545726hg38UCSC Ensembl
chr13:112197985..112198073hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16280951
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4734152
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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